24 hour allergy

Orange BookUNIISPLATC R06AE

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerMeijer Distribution Inc

CountryUS (United States)

ATC codeR06AE

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

ndc11
4125045839
1 BOTTLE in 1 CARTON (41250-458-39) / 30 TABLET, FILM COATED in 1 BOTTLE
ndc11
4125045866
14 BLISTER PACK in 1 CARTON (41250-458-66) / 1 TABLET, FILM COATED in 1 BLISTER PACK
ndc11
4125045875
2 BOTTLE in 1 CARTON (41250-458-75) / 45 TABLET, FILM COATED in 1 BOTTLE
ndc11
4125045887
1 BOTTLE in 1 CARTON (41250-458-87) / 300 TABLET, FILM COATED in 1 BOTTLE
ndc11
4125045895
1 BOTTLE in 1 CARTON (41250-458-95) / 45 TABLET, FILM COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)

64O047KTOA

CETIRIZINE HYDROCHLORIDE

RxCUI 203150

Orange Book

A078336

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "64O047KTOA",
    "rxcui": "203150",
    "inchikey": "PGLIUCLTXOYQMV-UHFFFAOYSA-N",
    "display_name": "CETIRIZINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "53ca807b-3ec2-4b5e-aa5a-6dcb756bb423": {
      "match": "brand_token",
      "title": "24 7 RELIEF AND RECOVERY PAIN RELIEVING (MENTHOL, UNSPECIFIED FORM) CREAM [TRIPLICARE INC]",
      "spl_version": "1",
      "published_date": "2026-05-06"
    }
  },
  "productid": "41250-458_18b74fff-8596-4050-93ee-4f15e6811de4",
  "productndc": "41250-458",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "078336",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Dec 27, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Dec 27, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "5MG",
        "product_no": "003",
        "approval_date": "Dec 27, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "004",
        "approval_date": "Dec 27, 2007"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CETIRIZINE HYDROCHLORIDE",
  "proprietary_name": "24 hour allergy",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078336",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Cetirizine Hydrochloride",
  "start_marketing_date": "19970707",
  "active_numerator_strength": "10"
}

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